drugset / Trial / NCT04060758

Open Label, Sequential-dose Study of PA5108 Latanoprost FA SR Ocular Implant for Mild-moderate Glaucoma

NCT04060758

Phase 1 Completed 37 enrolled PolyActiva Pty Ltd
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a multi-centre, open label, interventional, comparative, phase I study to identify a safe and efficacious dose (within the range of 14.7mcg to 35.5 mcg) of PA5108 (PolyActiva product code) Latanoprost free acid (FA) sustained release (SR) Ocular Implant in adults who have Primary Open Angle Glaucoma.

Timeline

Start
2020-03-11
Primary completion
2025-05-13
Completion
2025-05-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Latanoprost Small molecule 14.7 ug Other
Subject Latanoprost Small molecule 26.6 ug Other
Subject Latanoprost Small molecule 35.5 ug Other

Indications